A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737273



Internal ID160939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118354271..118358574hg38UCSC Ensembl
chrX:117488234..117492537hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg384304
hg194304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430321
Supporting Variants
Samples
Known GenesWDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737273
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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